|
 |
|

 |
|
Introduction |
Immune Thrombocytopenic Purpura (ITP) is a disorder of the blood.
Immune refers to the immune system's involvement in this
disorder. Antibodies, part of the body's immunologic defense
against infection, attach to blood platelet, cells that help stop
bleeding, and cause their destruction. Thrombocytopenia refers
to decrease in blood platelet. Purpura refers to the purplish-
looking areas of the skin and mucous membranes (such as the
lining of the mouth) where bleeding has occurred as a result of
decreased platelet.
Some cases of ITP are caused by drugs, and others are
associated with infection, pregnancy, or immune disorders such as
systemic lupus erythematosus. About half of all cases are
classified as "idiopathic," meaning the cause is unknown.
|
What Are the Symptoms of ITP? |
The main symptom is bleeding, which can include bruising
("ecchymosis") and tiny red dots on the skin or mucous membranes
("petechiae"). In some instances bleeding from the nose, gums,
digestive or urinary tracts may also occur. Rarely, bleeding
within the brain occurs.
|
How Is ITP Diagnosed? |
The physician will take a medical history and perform a thorough
physical examination. A careful review of medications the
patient is taking is important because some drugs can be
associated with thrombocytopenia. A complete blood count will be
done. A low platelet count will establish thrombocytopenia as
the cause of purpura. Often the next procedure is a bone marrow
examination to verify that there are adequate platelet-forming
cells (megakaryocyte) in the marrow and to rule out other
diseases such as metastatic cancer (cancer that has spread to the
bone marrow) and leukemia cancer of the blood cells themselves).
Another blood sample may be drawn to check for other conditions
sometimes associated with thrombocytopenia such as lupus and
infection.
Acute and Chronic Form of Thrombocytopenic Purpura
Acute (temporary) thrombocytopenic purpura is most commonly seen
in young children. Boys and girls are equally affected.
Symptoms often, but do not necessarily, follow a viral
infection. About 85 percent of children recover within 1 year
and the problem doesn't return.
Thrombocytopenic purpura is considered chronic when it has
lasted more than 6 months. The onset of illness may be at any
age. Adults more often have the chronic disorder and females are
affected two to three times more than males. The onset of
illness may be at any age.
|
How Is ITP Treated? |
If the doctor thinks a drug is the cause of the thrombocytopenia,
standard treatment involves discontinuing the drug's use.
Infection, if present, is treated vigorously since control of the
infection may result in a return of the platelet count to normal.
The treatment of idiopathic thrombocytopenic purpura is
determined by the severity of the symptoms. In somed from the
National Organization for Rare Disorders at P.O. Box 8923, New
Fairfield, CT 06812; tel: (203) 746-6518.
U.S. Department of Health and Human Services
Public Health Service
National Institutes of Health
National Heart, Lung, and Blood Institute
This e-text is not copyrighted. NIDDK encourages users to duplicate and distribute as many copies as needed.
|
|
|

|
NIH Publication No. 90-2114
September 1990
e-text last updated: 12 February 1998
|
|
|